Sucrase-isomaltase deficiency in humans. Different mutations disrupt intracellular transport, processing, and function of an intestinal brush border enzyme.-Reference-Cited by-同舟云学术

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Sucrase-isomaltase deficiency in humans. Different mutations disrupt intracellular transport, processing, and function of an intestinal brush border enzyme.

Published:1988-08-01 Issue:2 Volume:82 Page:667-679
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Naim H Y,Roth J,Sterchi E E,Lentze M,Milla P,Schmitz J,Hauri H P

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Cited by 113 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic and acquired sucrase‐isomaltase deficiency: A clinical review;Journal of Pediatric Gastroenterology and Nutrition;2024-02-08

2. The genetics of monogenic intestinal epithelial disorders;Human Genetics;2022-11-23

3. Loss of Sucrase-Isomaltase Function Increases Acetate Levels and Improves Metabolic Health in Greenlandic Cohorts;Gastroenterology;2021-12

4. Rosa canina L. Can Restore Endoplasmic Reticulum Alterations, Protein Trafficking and Membrane Integrity in a Dextran Sulfate Sodium-Induced Inflammatory Bowel Disease Phenotype;Nutrients;2021-01-29

5. Hypomorphic SI genetic variants are associated with childhood chronic loose stools;PLOS ONE;2020-05-20

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